Large Unit Red Cell Cryopreservation with Hydroxyethyl Starch'
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CRYOBIOLOGY 13, 500-506 (1976) Large Unit Red Cell Cryopreservation with Hydroxyethyl Starch’ E. D. ALLEN, L. WEATHERBEE, H. H. SPENCER, S. M. LINDENAUER, AND P. A. PERMOAD Medical Research, Veterans Administration Hospital and University of Michigan Medical Center, Ann Arbor, Michigan 48105 Red blood cells can be preserved by faster freezing and thawing rates than does freezing using either intra- or extracellular cryopreservation with intracellular agents agents. The most common intracellular such as glycerol. In general, this means agent, glycerol, is currently employed in freezing in liquid nitrogen and thawing in general use and provides clinically accepta- high temperature water baths, incorporat- ble red cells following post-thaw washing ing agitation of the unit at both points. It (13). would be advantageous if cells frozen with Extracellular agents do not enter the cell HES as the cryopreservative could be ad- during freezing. Therefore, red cells pre- ministered directly after thawing. This ar- served with these agents may be adminis- ticle describes results of freezing full units tered without post-thaw processing de- of red cells with HES as the cryoprotective pending on the agent used and the cell agent. preservation obtained. For example, poly- vinylpyrvolidone (PVP) and dextran re- MATERIALS AND METHODS ceived considerable attention as extracellu- Full units of whole blood (25 days old, lar agents but are currently considered collected in CPD) were centrifuged at 3000 unacceptable. PVP yields good cell pres- rpm for 15 min. After centrifugation, super- ervation but the molecular weight which natant plasma and buffy coat were re- affords the best cryopreservation is retained moved. In experiments using “washed for long periods in the reticuloendothelial cells” the packed red cells following cen- system ( 12 ). Dextran is unacceptable be- trifugation were mixed with an equal vol- cause it does not yield adequate cell pres- ume ‘of 0.9% NaCl and the centrifugation ervation. Hydroxyethyl starch (HES) pos- and removal of supernatant solution were sesses many of the characteristics required repeated two additional times. of an acceptable extracellular cryoprotec- The starch used in all experiments was a tive agent since it yields high cell recov- 40% aqueous solution containing 0.9% eries and is nonantigenic (7) and nontoxic NaCl prepared from powder (Lot No. (3, 10). A high molecular weight HES is PlPO05, McGaw Laboratories, Glendale, currently in use as a plasma expander. Calif. ). The final concentration of starch in Red cell cryopreservation utilizing HES the freezing mixture was 14% obtained by and other extracellular agents requires adding 35 parts of the 40% starch solution to 65 parts of the red cell mixture. In order Received October 24, 1975. to obtain a hematocrit near 40%, the un- 1 Supported in part by Office of Naval Research, Department of the Navy (Contract No. NAonr- washed packed red cells or the 0.9% NaCl 8-75). washed red cells were diluted with plasma 500 Copyright 1976 by Academic Press, Inc. All rights o6 reproduction in any form reserved. RED CELL CRYOPRESERVATION WITH HES 501 or 0.9 NaCl, respectively, before addition TABLE 1 of the 40% starch. Examination of Large Units of Red Cells Frozen Freezing mixtures (385-400 ml) were with 14y0 Hydroxyethyl Starcha frozen and thawed in Hemoflex bags (Style Parameter Prefreeae Post-thaw examined” mean 7450-2, Union Carbide Corp. ) placed in an f standard deviation aluminum holder. The aluminum holder containing the blood bag was kept at 4°C Cell R.ecover) for l-2 hr before freezing. Freezing was (%I 99.4 f 0.3 96.9 & 0.7 done by immersing in liquid nitrogen and Saline St#abilitJ (%:) 99.0 * 0.8 83.4 z!z 3.2 agitating at 200 cpm for 1 min followed by Supernatant Hb 150 cpm for an additional minute using a bg%) - 568 + 124.4 Linde BP2 blood processing unit. This two- Supernat,ant K + step method of agitation was found effec- bes/l) 9.2 f 2.8 37.6 f 2.1 tive in reducing the amount of Hemoffex Supernatant Na+ bes/l) 164.5 f 5.1 76.8 f 2.9 bag breakage (evidenced during thaw). ATP WI/g Hb) 3.1.5 f 0.29 2.06 f 0.34 After freezing, the bag was stored in its 2-3-DPG holder in liquid nitrogen vapor ( - 140°C) (&g Hb) 11.1.: f 1.96 8.73 f 2.22 until thawed (usually 16-24 hr). Thawing was ,done by immersion of the holder and ‘I Volume of freezing mixture 385400 ml ; red cell hematocrit near 40”/;, (3844); plasma present in bag in water (4749°C) using the Linde freezing mixture. machine at 170 cpm. The units were re- bN = 28. moved from the water bath when the freez- ing mixture was completely thawed and available kits (Sigma Chemical Corp., St. had reached a temperature of 5-15°C (usu- Louis, Missouri). ally 60-70 set). Red cells examined by electron micros- The parameters used to examine the red copy were fixed in a combination of gluta- cells before and after freezing included cell raldehyde and paraformaldehyde (4). Fol- recovery, .saline stability, and supernatant lowing fixation (1.5 hr, room temperature) hemoglobin, which have been previously de- the cells were washed in 0.1 M sodium scribed (14). Determination ‘of red cell cacodylate, pH 7.4 and postfixed in 1% ATP level was done enzymatically by mea- osmium tetroxide in 0.1 M sodium caco- suring the decrease in optical density of dylate (1 hr, 4°C). After alcoholic dehy- DPNH undergoing oxidation. The reaction dration the cells were transferred to propyl- which involves two steps utilizes 3-PGA ene oxide and embedded in Epon accord- and DPNH as substrates and phospho- ing to Luft (6). Silver-gray sections were glyceric phosphokinase and glyeraldehyde cut on a Sorvall MT-2 microtome and phosphate dehydrogenase as enzymes. The stained with 2% uranyl acetate and lead method is not specific for ATP and will citrate (11). Sections were examined and measure other nucleoside triphosphates if photographed with a Hitachi lla electron present. Determination of 2,3-DPG was microscope operated at 75 kV. also done enzymatically by measuring RESULTS changes of DPNH oxidation. The reaction involves three steps and utilizes ATP and Large Unit Freezing DPNH as substrates and 2,3-DPG phospha- The results of freezing large units (385- tase, phosphoglycerate kinase, and glycer- 400 ml final mixture) of red cells with hy- aldehyde phosphate dehydrogenase as en- droxyethyl starch (HES) are summarized zymes, Both ATP and 2,3-DPG determina- in Table 1. Cell recoveries are 97% (96.9 tions werle conducted using commercially -t 0.7) saline stabilities above 80% (83.4 502 ALLEN ET AL. TABLJS 2 Examination of Large Units of Red Cells Frozen with 14% Hydroxyet,hyl Starch 24 and 48 Hr after Thawa Parameter examined* Pr‘3frWZe TbZtW Post-thaw Mean standard deviation 24 hr 48 hr Cell Recovery (%) 99.6 f 0.3 97.2 f 0.4 96.7 f 0.54 96.3 + 0.7 Saline Stability (yc) 99.2 f 0.6 83.1 & 3.4 81.5 ZtI 2.9 81.1 & 2.4 Supernatant Hb (mg’%) - 530 f 82.8 622 It 101.6 698 f 96.4 Supernatant Kf (meq/l) 9.3 f 3.0 37.6 f 1.9 38.6 31 2.1 39.2 zt 1.7 Supernatan t Na + (meq/l) 164.1 * 5.5 77.5 f 2.8 77.4 f 3.4 77.2 zt 3.8 ATP (W/g Hb) 3.16 f 0.38 2.08 f 0.34 2.09 f 0.65 2.04 + 0.51 2-3 DPG (&&M/g Hb) 11.42 f 1.80 8.89 41 2.30 7.32 f 2.54 5.24 f 2.40 a Red cell hematocrit of freezing mixture near 40y0 (39-44), total volume of freezing mixture 38.5400 ml, units stored at, 4OC following thaw. bN = 22. * 3.2) and levels of supernatant hemo- unchanged, and the levels of 2,3-DPG de- globin at 570 mg% (568 -+ 124). Potas- crease. sium leaves the cells during a freeze-thaw We have previously reported that the pres- cycle increasing in the external solution ence of plasma lowered the saline stability from 9.2 meq/l in the prefreeze blood to of small units of red cells (30 ml freezing 37.5 meq/l at thaw. ATP and 2,3-DPG mixtures) frozen with HES but had no levels drop approximately 30 and 20%, effect on the cell recoveries or levels of respectively, when compared to the blood supernatant hemoglobin ( 14). To deter- as received. Plasma is added to the units mine whether a similar effect was observed of packed cells to ensure a final red cell with large units ‘of red cells under the con- hematocrit near 40% (Table 1). ditions used here, units were washed with Only moderate changes ‘occur after thaw 0.9% NaCl to remove plasma. Saline was when the cells are stored at 4°C (Table 2). added to the cells following centrifugation After 48 hr, the cell recoveries remain near to adjust the hematocrit to near 40%. Com- 96% (96.3 I 0.7) with the saline stabilities pared to the units frozen with unwashed still above 80% (81.1 * 2.4). The levels of cells (Tables 1 and 2), the various param- supernatant hemoglobin increase 150 to 700 eters examined at thaw with the prefreeze mg%; ATP and potassium remain nearly washed cells are nearly the same (Table 3).